BAZ1B antibody
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- Target See all BAZ1B Antibodies
- BAZ1B (Bromodomain Adjacent To Zinc Finger Domain, 1B (BAZ1B))
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Reactivity
- Human, Mouse, Rat
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Host
- Rabbit
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Clonality
- Polyclonal
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Conjugate
- This BAZ1B antibody is un-conjugated
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Application
- Western Blotting (WB), Immunohistochemistry (IHC)
- Purification
- Affinity purification
- Immunogen
- Recombinant protein of human BAZ1B
- Isotype
- IgG
- Top Product
- Discover our top product BAZ1B Primary Antibody
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- Application Notes
- WB 1:500 - 1:2000 IHC 1:50 - 1:200
- Restrictions
- For Research Use only
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- Concentration
- 1 mg/mL
- Buffer
- Buffer: PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3.
- Preservative
- Sodium azide
- Precaution of Use
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- Storage
- -20 °C
- Storage Comment
- Store at -20°C. Avoid freeze / thaw cycles.
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- Target
- BAZ1B (Bromodomain Adjacent To Zinc Finger Domain, 1B (BAZ1B))
- Alternative Name
- BAZ1B (BAZ1B Products)
- Synonyms
- BAZ1B antibody, wstf antibody, wbscr9 antibody, wbscr10 antibody, LOC100220420 antibody, WBSCR10 antibody, WBSCR9 antibody, WSTF antibody, C87820 antibody, Wbscr9 antibody, fi60d02 antibody, im:7137554 antibody, wu:fi60d02 antibody, bromodomain adjacent to zinc finger domain 1B antibody, bromodomain adjacent to zinc finger domain, 1B antibody, bromodomain adjacent to zinc finger domain 1B S homeolog antibody, BAZ1B antibody, baz1b antibody, Baz1b antibody, baz1b.S antibody
- Background
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Synonyms: Bromodomain Adjacent To Zinc Finger Domain 1B,Williams-Beuren Syndrome Chromosomal Region 10 Protein,Williams-Beuren Syndrome Chromosomal Region 9 Protein,Williams Syndrome Transcription Factor,Transcription Factor WSTF,EC 2.7.10.2,WBSCR10,WBSCR9.
Background: This gene encodes a member of the bromodomain protein family. The bromodomain is a structural motif characteristic of proteins involved in chromatin-dependent regulation of transcription. This gene is deleted in Williams-Beuren syndrome, a developmental disorder caused by deletion of multiple genes at 7q11.23.
- Molecular Weight
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Observed_MW: 190kDa
Calculated_MW: 170kDa
- Gene ID
- 9031
- UniProt
- Q9UIG0
- Pathways
- Nuclear Hormone Receptor Binding, Chromatin Binding
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